HCID 21393838, compound → HCID 20523201, compound
Reaction equation
[N+:1]([C:4]1[C:13]([C:14]([F:17])([F:16])[F:15])=[C:12]2[C:7]([CH:8]=[CH:9][N:10]=[CH:11]2)=[CH:6][CH:5]=1)([O-])=O>[Zn].C(O)(=O)C>[NH2:1][C:4]1[C:13]([C:14]([F:17])([F:15])[F:16])=[C:12]2[C:7]([CH:8]=[CH:9][N:10]=[CH:11]2)=[CH:6][CH:5]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Reducing the 7-nitro group of 7-nitro-8-trifluoromethylisoquinoline with zinc and acetic acid by the procedure of Example 17 gives 7-amino-8-trifluoromethylisoquinoline. Hydrogenating by the procedure of Example 9 gives 7-amino-8-trifluoromethyl-1,2,3,4-tetrahydroisoquinoline.
Sources & evidence
- ORD record
- ord-99ed1f1403c6431d8f5f01a7d99a88aa
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03988339
Reaction notes
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